A small synthetic peptide-like molecule designed to mimic waglerin-1, a toxin in the venom of Wagler’s pit viper that blocks the muscle receptor for acetylcholine, the nerve signal that makes muscles contract. It’s marketed to soften expression lines.
Evidence. Human data are the maker’s unpublished 28-day cream test in 45 volunteers and two industry studies of a serum mixing it with Argireline and other actives (50 women for 12 weeks and 42 for 8 weeks, no placebo group), so its own effect hasn’t been shown. Cosmetics don’t need FDA approval.
What it’s used for
None of these uses is approved. Uses tested in people come first, then claims that rest on animal studies or user reports.
Expression lines and wrinkles
TrialUnproven alone: in the maker’s unpublished 28-day test (45 volunteers), roughness fell 21% and wrinkle depth 20% (top single result 52%); industry studies tested only serums mixing it with other actives.
A “Botox-like” or “snake venom” wrinkle relaxer
AnimalUnproven: it mimics a viper-venom toxin, and in the maker’s lab tests it cut contractions of nerve-connected muscle cells by 82%. No study shows it relaxes facial muscles through skin.
Alongside botulinum toxin injections
CommunityUntested: clinicians in an industry-supported case report pair a serum containing it with toxin injections; no controlled study has measured any added benefit.
Injections for wrinkles
No studyUnproven: no study has tested Syn-Ake by injection in people or animals, and cosmetic-grade peptide isn’t made to injectable standards.
Trial: tested in people, with the result. Animal: cell or animal studies only. Community: reported by users, not studied. No study: nothing published supports it.
Not approved as a drug in the US or EU; used as a cosmetic ingredient. Cosmetics don’t need FDA approval before sale.
US compounding
Never nominated for FDA’s compounding bulk lists; it isn’t on any of FDA’s 503A or 503B category lists (May 2026 and March 2025 versions).
European Union
No marketing authorization as a medicine. Listed in the EU cosmetic ingredient database (CosIng) as dipeptide diaminobutyroyl benzylamide diacetate, a skin-conditioning ingredient, with no annex restriction.
United Kingdom
No marketing authorization (MHRA). Cosmetics containing it fall under UK cosmetics law rather than medicines regulation.
Canada
No marketing authorization; no product lists it as an active ingredient in Health Canada’s Drug Product Database.
Australia
No marketing authorization, and it isn’t named in the Poisons Standard (October 2026).
Sport (WADA 2026)
Not banned in sportNot named on the 2026 list. It’s a topical cosmetic ingredient, not a drug of the kind S0 covers.
Category 2 is FDA’s list of bulk substances that may present significant safety risks in compounding. The 503A bulks list adds substances that pharmacies may compound with. Advisory committee votes are advice; FDA makes the final decision. Sport status follows the WADA Prohibited List in force since January 1, 2026; athletes should confirm with their anti-doping organization. Checked October 5, 2026. Status outside the US checked October 7, 2026 against EMA, MHRA, Health Canada and TGA records. By country: EU, UK, Canada, Australia. Status of every compound.
How it works
Syn-Ake is a small synthetic molecule built from beta-alanine, proline and diaminobutyric acid, designed to mimic waglerin-1, a viper-venom toxin that blocks the muscle nicotinic acetylcholine receptor, the switch nerve signals use to make muscle contract. In the maker’s lab tests it reduced contractions of nerve-connected muscle cells by 82% after 2 hours, an effect described as reversible. No published study shows it reaches facial muscle through skin.
AnimalMainly from cell and animal studies; not shown in people.
Not known
Whether any reaches facial muscle through skin, and whether wrinkle changes in tests come from muscle effects rather than surface effects such as moisture, is unknown.
Protocol
Trial
Supplier data
Maker’s test: cream with 4% of the supplier solution (about 80–120 ppm peptide), twice daily for 28 days in 45 volunteers.
Community
Finished products contain 1–4% of the supplier solution, about 20–120 ppm peptide; “4% Syn-Ake” doesn’t mean 4% pure peptide.
Frequency
Twice daily (topical)
Route
Topical only
Cycle
Continuous; tests judged results at 28 days to 12 weeks.
Week 15913172125
Continuous, shown over 26 weeks
Common protocols
The ways Syn-Ake is most often run, each tagged with where it comes from.
Finished cream or serum
Community
Dose
1–4% supplier solution (about 20–120 ppm peptide)
How often
Twice daily
How long
Judge at 4–8 weeks
The supplier solution is only about 0.25% peptide. It’s added to a finished product at cool-down (below 40 °C), never used neat.
Maker’s test
Trial
Dose
4% supplier solution in a cream
How often
Twice daily
How long
28 days
45 volunteers split across placebo, a 10% Argireline product and 4% SYN-AKE: roughness fell 21% and wrinkle depth 20% from day 0 (Argireline: 4% and 2%). The much-quoted 52% was one volunteer’s top result.
Taking it
Where it goes
Applied to clean skin over expression lines, such as the forehead and around the eyes. Topical only; never inject it.
If you miss a dose
Nothing special. Skip it and use the next application as usual.
Maker’s test in 45 volunteers: roughness 21% and wrinkle depth 20% lower than at day 0, and up to 52% on one volunteer’s forehead. Supplier data only, unpublished.
Trial
12 weeks
With a serum mixing it with Argireline and other actives, wrinkle scores improved 35–69% from baseline in 50 women, with no comparison group (Zhu 2026).
Trial
Side effects and what to do
Skin irritation or redness
Patch-test first. Stop if it doesn’t settle.
No adverse events in two 8–12-week studies of a serum containing it (92 women)
Studies were small and tested mixes, so rare reactions can’t be ruled out.
Eye irritation
Keep it out of the eyes. Rinse with water if it gets in.
Stop and get medical help
Stop and see a doctor for a spreading rash, swelling, blistering or hives, eye pain after contact, or any new muscle weakness.
Can it cause …?
The side effects people ask about most, answered one by one. Each answer says where it comes from.
Acne, rash or skin changes
TrialNo adverse events were reported in two 8–12-week studies of a serum containing it (92 women); its own skin-safety data aren’t published.
Cancer risk
No dataNo cancer data in people or animals; the only human studies lasted up to 12 weeks and tested mixes.
TirednessHeadacheNausea or vomitingDiarrhea or constipationDizzinessTrouble sleepingHair lossWater retention or swellingJoint or muscle painAnxiety, low mood or irritabilityLow or high blood sugarFast heartbeat or blood pressure changesMore hungerLiver strainKidney problems
Not reportedNot reported in two single-group studies of a serum containing it (50 and 42 women, 8–12 weeks), which saw no adverse events.
Trial: reported in human studies. Not reported: studied in people and not reported. No data: no human safety data. A side effect that hasn’t been reported can still happen, especially with long or high-dose use. Any of these across every compound: the side-effect finder.
Who should avoid it
No product label covers Syn-Ake, so these come from human studies and from precautions based on how it works. Most important first.
Anyone thinking of injecting it
PrecautionIt is a cosmetic ingredient, not made to injectable standards, and has never been tested by injection. It isn’t botulinum toxin or snake venom.
Anyone mixing pure powder at high strength
PrecautionThe maker’s test level works out to about 80–120 ppm peptide; stronger mixes haven’t been tested for benefit or safety.
People with myasthenia gravis or similar conditions
PrecautionIt is designed to block the muscle acetylcholine receptor, the signal impaired in myasthenia gravis. Skin absorption hasn’t been measured, and use in these conditions hasn’t been studied.
Pregnancy or breastfeeding
PrecautionNo human safety data exist.
Interactions
No interaction studies have been published, and no product label lists any. Clinicians have described pairing a serum containing it with botulinum toxin injections, but only in an industry-supported case report.
Precaution: follows from how it works or from a related drug, and hasn’t been tested. This isn’t a complete list: a pharmacist or doctor can check a specific medicine or condition. Every documented interaction, by medicine: drug interactions.
Special situations
What’s known about pregnancy, breastfeeding, kidney and liver problems, age and surgery. Where nothing has been studied, the row says so.
Pregnancy
PrecautionNo human or animal data on pregnancy; Syn-Ake alone has never been tested in a published human study.
Breastfeeding
PrecautionNo human data; it isn’t known whether any reaches breast milk.
Kidney problems
PrecautionNot studied in people with kidney disease, and no study has measured how much passes through skin.
Liver problems
PrecautionNot studied in people with liver disease, and no study has measured how much passes through skin.
Older adults
PrecautionNot studied as a group; the serum studies enrolled women aged 25–55 and reported no age-specific safety data.
Children and teens
PrecautionNot studied in anyone under 18, and not approved for any age.
Surgery and anesthesia
PrecautionNo data; tell the surgical team about any compound used, including skin products meant to relax muscles.
Precaution: not studied, so the caution follows from how it works or from a related drug. Ages are given as approved or studied; this site never gives doses for children. Across every compound: pregnancy, breastfeeding, kidney disease, liver disease, older adults and surgery.
Paired in commercial serums as two different “Botox-like” peptides; tested together only in uncontrolled industry studies.
Human studies
The published human study we found, with how many people took part. Animal studies aren’t listed here.
202692 people
Static wrinkle scores improved 35–69% and dynamic wrinkle scores 10–13% from baseline (p<0.001), with no adverse events; with no comparison group, Syn-Ake’s share is unknown.
Design
Two single-group studies without placebo (50 and 42 completers), run by a cosmetics company’s researchers
Dose
Serum with acetyl hexapeptide-8, dipeptide diaminobutyroyl benzylamide diacetate, gluconolactone, niacinamide and kelp extract, twice daily
Length
12 weeks (static wrinkles) and 8 weeks (dynamic wrinkles)
No ongoing trial of Syn-Ake is registered, and none has finished recently without publishing its results. Checked on ClinicalTrials.gov, October 7, 2026. Every compound: trials under way.
Limits of the evidence
Syn-Ake’s human evidence is the maker’s unpublished 28-day test in 45 volunteers and two industry studies of a serum mixing it with Argireline and other actives (50 and 42 women, 8–12 weeks, no comparison group). No peer-reviewed controlled trial of it alone exists. Its muscle-relaxing action comes only from the maker’s cell tests, and skin absorption hasn’t been measured. Pure-powder mixes, long-term use and injection are untested.
Serum strength
Syn-Ake is used on the skin, so the math is a dilution, not a syringe dose.
Powder
Serum volume
Strength
Percent
ppm
10 mg
50 mL
0.2 mg/mL
0.02%
200 ppm
10 mg
100 mL
0.1 mg/mL
0.01%
100 ppm
10 mg
200 mL
0.05 mg/mL
0.005%
50 ppm
10 mg
500 mL
0.02 mg/mL
0.002%
20 ppm
The maker supplies it as a glycerin and water solution with about 0.2–0.3% peptide. Its 4% test level equals about 80–120 ppm, roughly 10 mg of pure peptide in 100 mL of serum.
Datasheet
Half-life
No reliable value has been published.
Type
Peptide, 3 amino acids
Molecular weight
495.6 g/mol
Formula
C23H37N5O7
Sequence
(β-Ala)-P-(Dab)-NH-benzyl2 acetate
Storage before use
Supplier solution: sealed, away from light, at 15–25 °C (stable at least 2 years, per the maker). Pure powder: freezer (about −20 °C), kept dry.
After mixing or opening
The supplier solution has no preservative, and the maker says to use an opened container right away. Finished serum: cool and dark.
Molecule: PubChem CID 71465152 (diacetate salt; free base C19H29N5O3, about 375.5); CAS 823202-99-9; UNII 38H206R00R
Storage:Community Maker’s technical brochure for the supplier solution; common research-peptide practice for powder
Dipeptide diaminobutyroyl benzylamide diacetate (INCI); H-β-Ala-Pro-Dab-NH-benzyl; some reviews call it tripeptide-3, an INCI name that belongs to a different peptide
Brand names
SYN-AKE is the ingredient’s trade name; no drug product exists
First described
Developed by a Swiss cosmetic-ingredient maker as a small mimic of waglerin-1, a viper-venom peptide.
The maker supplies a glycerin and water solution with about 0.2–0.3% peptide, used at 1–4%, so finished products hold roughly 20–120 ppm. Pure powder is hundreds of times stronger than that solution.
Cautions
Cosmetic ingredient; never inject it. It isn’t botulinum toxin or snake venom.
Don’t use pure powder at “1–4%”. That figure refers to the dilute supplier solution.
Its muscle-relaxing action comes only from the maker’s cell tests; no study shows it reaches facial muscle.
Patch-test first and keep it out of the eyes.
Questions
What is Syn-Ake?
A small synthetic peptide-like molecule designed to mimic waglerin-1, a toxin in the venom of Wagler’s pit viper that blocks the muscle receptor for acetylcholine, the nerve signal that makes muscles contract. It’s marketed to soften expression lines.
How does Syn-Ake work?
Syn-Ake is a small synthetic molecule built from beta-alanine, proline and diaminobutyric acid, designed to mimic waglerin-1, a viper-venom toxin that blocks the muscle nicotinic acetylcholine receptor, the switch nerve signals use to make muscle contract. In the maker’s lab tests it reduced contractions of nerve-connected muscle cells by 82% after 2 hours, an effect described as reversible. No published study shows it reaches facial muscle through skin. Whether any reaches facial muscle through skin, and whether wrinkle changes in tests come from muscle effects rather than surface effects such as moisture, is unknown.
Is Syn-Ake FDA-approved?
Not approved as a drug in the US or EU; used as a cosmetic ingredient. Cosmetics don’t need FDA approval before sale. Never nominated for FDA’s compounding bulk lists; it isn’t on any of FDA’s 503A or 503B category lists (May 2026 and March 2025 versions).
What is the usual Syn-Ake dose?
From human studies (Supplier data): Maker’s test: cream with 4% of the supplier solution (about 80–120 ppm peptide), twice daily for 28 days in 45 volunteers. From community reports, not established: Finished products contain 1–4% of the supplier solution, about 20–120 ppm peptide; “4% Syn-Ake” doesn’t mean 4% pure peptide. These are the amounts sources reference, not recommendations.
Who should avoid Syn-Ake?
No product label covers Syn-Ake, so these come from human studies and from precautions based on how it works. Anyone thinking of injecting it: It is a cosmetic ingredient, not made to injectable standards, and has never been tested by injection. It isn’t botulinum toxin or snake venom. Anyone mixing pure powder at high strength: The maker’s test level works out to about 80–120 ppm peptide; stronger mixes haven’t been tested for benefit or safety. People with myasthenia gravis or similar conditions: It is designed to block the muscle acetylcholine receptor, the signal impaired in myasthenia gravis. Skin absorption hasn’t been measured, and use in these conditions hasn’t been studied. The “Who should avoid it” section lists 1 more group.
How should Syn-Ake be stored?
Supplier solution: sealed, away from light, at 15–25 °C (stable at least 2 years, per the maker). Pure powder: freezer (about −20 °C), kept dry. The supplier solution has no preservative, and the maker says to use an opened container right away. Finished serum: cool and dark. This is common practice; no product label covers it.
Is Syn-Ake banned in sport?
No. Not named on the 2026 list. It’s a topical cosmetic ingredient, not a drug of the kind S0 covers.
Has Syn-Ake been studied in people?
Yes. The human studies section lists one published study. The largest, from 2026, included 92 people. Static wrinkle scores improved 35–69% and dynamic wrinkle scores 10–13% from baseline (p<0.001), with no adverse events; with no comparison group, Syn-Ake’s share is unknown.
How long has Syn-Ake been studied in people?
Trial 12 weeks, in a single-group study of a serum mixing it with other actives (50 women). Alone, only the maker’s 28-day test.
Is Syn-Ake ever injected or taken by mouth?
Trial Sold for creams and serums, but no study has measured how much passes through skin. Human data come only from serums mixing it with other actives; injection is untested.
What happens if you use too much Syn-Ake?
No study There’s no label and no overdose data, and Syn-Ake alone has never been tested in a published human study. Call Poison Help (1-800-222-1222), or emergency services for severe symptoms.
Sources
Maker’s technical brochure for SYN-AKE: muscle-cell test and 28-day test in 45 volunteers (unpublished, undated)
Errante et al., cosmeceutical peptides review, summarizing the maker’s Syn-Ake data (Front Chem 2020) PMID 33195061
Zhu et al., ex vivo and two 8–12-week studies of a serum with acetyl hexapeptide-8 and dipeptide diaminobutyroyl benzylamide diacetate (Int J Cosmet Sci 2026) PMID 41668671
Debono et al., origin of the viper-venom waglerin peptides used in anti-wrinkle creams (J Mol Evol 2017) PMID 27864608
For the protocol details
Maker’s technical brochure for SYN-AKE, muscle-cell and 45-volunteer tests (unpublished)
For how it works, who should avoid it and the limits of the evidence
Maker’s technical brochure for SYN-AKE, muscle-cell contraction test (unpublished)
McArdle et al., waglerin-1 blocks the adult form of the muscle nicotinic acetylcholine receptor (J Pharmacol Exp Ther 1999) PMID 10087048
Lupin et al., clinicians’ experience with a peptide serum alongside botulinum toxin injections (J Drugs Dermatol 2024) PMID 39496132
For uses, the side-effect questions, special situations, trials, identifiers and status outside the US
Maker’s technical brochure for SYN-AKE: supplied form, muscle-cell test and 28-day test in 45 volunteers (unpublished)
Schagen, topical peptide review, citing the maker’s 4% and 52% figures (Cosmetics 2017) doi:10.3390/cosmetics4020016
FDA Global Substance Registration System record (UNII 38H206R00R); PubChem CID 71465152; WHO ATC index (no entry)
EU CosIng entries for dipeptide diaminobutyroyl benzylamide diacetate and tripeptide-3 (checked October 8, 2026)
Health Canada Drug Product Database search (checked October 8, 2026)
Australian Poisons Standard, October 2026 (no entry)
ClinicalTrials.gov searches for Syn-Ake and dipeptide diaminobutyroyl (no registered trials; checked October 8, 2026)
Doses tagged Community come from public dosing guides and user reports, checked against at least two of them. Those sites aren’t named here because many of them sell peptides or earn commissions on them.